Evidence map›Paper›PMID 31089211›Full record

ArticleScientific reports2019

DEEPred: Automated Protein Function Prediction with Multi-task Feed-forward Deep Neural Networks.

Ahmet Sureyya Rifaioglu, Tunca Doğan, Maria Jesus Martin, Rengul Cetin-Atalay, Volkan Atalay

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
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  6. Article
  7. Multitask Learning-Based Approaches for Protein Function Prediction.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  8. Article
  9. ProT-GFDM: A generative fractional diffusion model for protein generation.Computational and structural biotechnology journal · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Mutual annotation-based prediction of protein domain functions with Domain2GO.Protein science : a publication of the Protein Society · 2024
    Article
  17. Review
  18. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ahmet Sureyya RifaiogluDepartment of Computer Engineering, METU, Ankara, 06800, Turkey.ORCID http://orcid.org/0000-0001-6717-4767
Tunca DoğanEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, Cambridge, CB10 1SD, UK. tdogan@ebi.ac.uk.
Maria Jesus MartinEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, Cambridge, CB10 1SD, UK.
Rengul Cetin-AtalayKanSiL, Department of Health Informatics, Graduate School of Informatics, METU, Ankara, 06800, Turkey.ORCID http://orcid.org/0000-0003-2408-6606
Volkan AtalayDepartment of Computer Engineering, METU, Ankara, 06800, Turkey. vatalay@metu.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Automated protein function prediction is critical for the annotation of uncharacterized protein sequences, where accurate prediction methods are still required. Recently, deep learning based methods have outperformed conventional algorithms in computer vision and natural language processing due to the prevention of overfitting and efficient training. Here, we propose DEEPred, a hierarchical stack of multi-task feed-forward deep neural networks, as a solution to Gene Ontology (GO) based protein function prediction. DEEPred was optimized through rigorous hyper-parameter tests, and benchmarked using three types of protein descriptors, training datasets with varying sizes and GO terms form different levels. Furthermore, in order to explore how training with larger but potentially noisy data would change the performance, electronically made GO annotations were also included in the training process. The overall predictive performance of DEEPred was assessed using CAFA2 and CAFA3 challenge datasets, in comparison with the state-of-the-art protein function prediction methods. Finally, we evaluated selected novel annotations produced by DEEPred with a literature-based case study considering the 'biofilm formation process' in Pseudomonas aeruginosa. This study reports that deep learning algorithms have significant potential in protein function prediction; particularly when the source data is large. The neural network architecture of DEEPred can also be applied to the prediction of the other types of ontological associations. The source code and all datasets used in this study are available at: https://github.com/cansyl/DEEPred .

Indexed as

Neural Networks, ComputerBacterial ProteinsBiofilmsData MiningDeep LearningGene OntologyHumansModels, BiologicalProteinsPseudomonas aeruginosaPseudomonas InfectionsSoftwareBacterial ProteinsProteins

Identifiers

PMID31089211
PMCPMC6517386

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.